Statistical Programmer Analyst I/II -Permanent Role-Hybrid @ Ontario Canada

Posted 6 Days Ago
Be an Early Applicant
Hiring Remotely in Ontario, ON, CAN
Remote or Hybrid
60-80 Annually
Mid level
Pharmaceutical
The Role
Develop, validate, and maintain statistical programs (TLFs) using SAS and R. Perform data manipulation, analysis, visualization, and QC. Collaborate with biostatisticians and data management, ensure CDISC and regulatory compliance, and support submission documentation.
Summary Generated by Built In

ClinChoice is a global full-service CRO committed to professional growth and a quality-driven “one-team” culture. We are seeking a Statistical Programmer Analyst I/II to join our in-house team and support projects across a diverse client portfolio, including pharmaceutical, biotechnology, medical device, and consumer health companies of varying sizes.

 

Job Summary:
We are seeking an experienced Statistical Programmer Analyst I/II with strong expertise in SAS programming to support clinical trial data analysis and reporting. The ideal candidate will have hands-on experience in developing, validating, and maintaining statistical outputs using R/SAS, along with a solid understanding of clinical data standards.

Key Responsibilities:
  • Develop, validate, and maintain statistical programs using SAS for the generation of Tables, Listings, and Figures (TLFs)
  • Perform data manipulation, analysis, and visualization using R/SAS and relevant packages
  • Collaborate with Biostatisticians and Data Management teams to support clinical study deliverables
  • Ensure compliance with regulatory standards and company SOPs
  • Conduct quality control (QC) and validation of programming outputs
  • Support submission activities and documentation as required

 

Required Skills & Qualifications:
  • Bachelor’s or Master’s degree in Statistics, Biostatistics, Computer Science, or a related field
  • 3+ years of experience in statistical programming within the pharmaceutical/biotech industry
  • Hands-on experience with R programming in a clinical trial environment is a plus.
  • Good understanding of R packages. 
  • Good understanding of CDISC standards (SDTM, ADaM)
  • Strong knowledge of clinical trial data and regulatory requirements
Preferred Qualifications:
  • Experience working in an FSP model or with global pharmaceutical clients
  • Exposure to submission activities (e.g., FDA/EMA)
  • Familiarity with SAS alongside R is a plus
  • Strong problem-solving and communication skills

 


Open Date: 7/16/2026

Close Date: 8/14/2026


ClinChoice Canada Inc. is proud to be an equal opportunity employer, valuing and respecting diversity.  We are committed to inclusive, barrier-free recruitment and selection processes. We will accommodate the needs of qualified applicants under the Human Rights Code and the Accessibility for Ontarians Disabilities Act, in all aspects of the hiring process, upon request by calling + 1 (647)724-5709 x 301. 

We thank all applicants for their interest; however, only those being considered for an interview will be contacted. In accordance with Federal Personal Information Protection and Electronic Documents Act ("PIPEDA") , personal information is collected under the authority of the Act and will only be used for candidate selection.

#LI-TT1 #LI-Remote #Senior#permanent

 

The base salary pay range represents the anticipated low and high range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. 

Canada Pay Range
$60$80 CAD

Skills Required

  • Bachelor's or Master's degree in Statistics, Biostatistics, Computer Science, or related field
  • 3+ years of experience in statistical programming within the pharmaceutical/biotech industry
  • Strong expertise in SAS programming for generation of Tables, Listings, and Figures (TLFs)
  • Good understanding of CDISC standards (SDTM, ADaM)
  • Strong knowledge of clinical trial data and regulatory requirements
  • Hands-on experience with R programming in a clinical trial environment
  • Experience working in an FSP model or with global pharmaceutical clients
  • Exposure to submission activities (e.g., FDA/EMA)
  • Familiarity with SAS alongside R
  • Strong problem-solving and communication skills

ClinChoice Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ClinChoice and has not been reviewed or approved by ClinChoice.

  • Flexible Benefits Flexible arrangements, including telecommuting and flextime with no core hours in some regions, are highlighted for many roles. Feedback suggests flexibility is commonly available but depends on role and location.
  • Leave & Time Off Breadth Vacation, personal, and sick days are part of the core package, with some markets granting paid leave from the date of hire. Feedback suggests time off is standard-to-decent across locations, though specifics vary.
  • Healthcare Strength Health coverage is positioned as a core benefit, with some accounts describing overall benefits as full or good. In the U.S., healthcare sits within a conventional CRO package alongside medical, dental, and vision.

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The Company
HQ: Fort Washington, PA
5,000 Employees
Year Founded: 1995

What We Do

ClinChoice is a global full-service Contract Research Organization (CRO) specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies, aiming to accelerate the development and commercialization of innovative drugs and devices.

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